HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94001816C= , CM000663.2:g.94001816C= | GRCh38 |
NC_000001.10:g.94467372C= , CM000663.1:g.94467372C= | GRCh37 |
NC_000001.9:g.94239960C= | NCBI36 |
NG_009073.1:g.124334G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000370225.4:c.6282+42G= MANE Select | ENSP00000359245.3:n.6282+42G= | |
ENST00000370225.3:c.6282+42G= | ENSP00000359245.3:n.6282+42G= | |
ENST00000465352.1:n.740G= | ||
ENST00000536513.5:c.2658+42G= | ENSP00000439707.2:n.2658+42G= | |
NM_000350.2:c.6282+42G= | NP_000341.2:n.6282+42G= | |
NM_000350.3:c.6282+42G= MANE Select | NP_000341.2:n.6282+42G= |